Evidence map›Paper›PMID 38982319›Full record

ArticleOrphanet journal of rare diseases2024

Unveiling the untreated: development of a database algorithm to identify potential Fabry disease patients in Germany.

Max J Hilz, Nicole Lyn, Felix Marczykowski, Barbara Werner, Marc Pignot, Elvira Ponce, Joseph Bender, Michael Edigkaufer, Pronabesh DasMahapatra

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Max J HilzUniversity of Erlangen-Nuremberg, Erlangen, Germany.
Nicole LynSanofi, Cambridge, MA, USA. Nicole.Lyn@sanofi.com.ORCID 0000-0001-9707-2446
Felix MarczykowskiOracle Life Sciences, Munich, Germany.
Barbara WernerTeam Gesundheit GmbH, Essen, Germany.
Marc PignotZEG Berlin - Center for Epidemiology and Health Research, Berlin, Germany.
Elvira PonceSanofi, Cambridge, MA, USA.
Joseph BenderSanofi, Cambridge, MA, USA.
Michael EdigkauferSanofi, Frankfurt, Germany.
Pronabesh DasMahapatraSanofi, Cambridge, MA, USA.

Funding

Sanofi NA
6 · The paper itself

Abstract

backgroundFabry disease (FD), an X-linked lysosomal storage disorder, is caused by mutations in the gene encoding α-galactosidase A, resulting in lysosomal accumulation of globotriaosylceramide and other glycosphingolipids. Early detection of FD is challenging, accounting for delayed diagnosis and treatment initiation. This study aimed to develop an algorithm using a logistic regression model to facilitate early identification of patients based on ICD-10-GM coding using a German Sickness Fund Database.

methodsThe logistic regression model was fitted on a binary outcome variable based on either a treated FD cohort or a control cohort (without FD). Comorbidities specific to the involved organs were used as covariates to identify potential FD patients with ICD-10-GM E75.2 diagnosis but without any FD-specific medication. Specificity and sensitivity of the model were optimized to determine a likely threshold. The cut-point with the largest values for the Youden index and concordance probability method and the lowest value for closest to (0,1) was identified as 0.08 for each respective value. The sensitivity and specificity for this cut-point were 80.4% and 79.8%, respectively. Additionally, a sensitivity analysis of the potential FD patients with at least two codes of E75.2 diagnoses was performed.

resultsA total of 284 patients were identified in the potential FD cohort using the logistic regression model. Most potential FD patients were < 30 years old and female. The identification and incidence rates of FD in the potential FD cohort were markedly higher than those of the treated FD cohort.

conclusionsThis model serves as a tool to identify potential FD patients using German insurance claims data.

Indexed as

AlgorithmsFabry DiseaseAdolescentAdultAgedDatabases, FactualFemaleGermanyHumansLogistic ModelsMaleMiddle AgedYoung AdultAlgorithmBKK German Sickness Fund DatabaseEarly diagnosisFabry diseaseLogistic regression modelling

Identifiers

PMID38982319
PMCPMC11234697

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.